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Becton Dickinson (BD) (CareFusion 303, Inc.) Recalls Alaris Pump Module Model 8100 Bezel Assembly Which Could Result in Free Flow, Over-Infusion, Under-Infusion, or Interruption of Infusion

The bezel posts may become cracked and separated which could lead to inaccurate delivery of fluids to the patient. From 2011-2017, the Alaris Pump Module Model 8100 was manufactured with a type of plastic called FR-110. The manufacturing process for the FR-110 plastic resulted in weakening of the plastic, which may lead to separation of the bezel post from the pumping mechanism or other damage to the bezel, such as cracking. Separation or cracking of bezel posts may lead to over-infusion, under-infusion, free-flow state, or interruption of infusion.

For more information visit: https://www.fda.gov/medical-devices/medical-device-recalls/becton-dickinson-bd-carefusion-303-inc-recalls-alaris-pump-module-model-8100-bezel-assembly-which?utm_campaign=2019-07-18%20Becton%20Dickinson%20%28BD%29%20Recalls%20Alaris%20Pump%20Module%20Model%208100%20Bezel%20Assembly&utm_medium=email&utm_source=Eloqua

 

 

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